NDC 71335-2916 – Acetaminophen and Codeine Phosphate

Acetaminophen 300 mg/1; Codeine Phosphate 30 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CIII

Product NDC71335-2916

Product details

Brand name
Acetaminophen and Codeine Phosphate
Generic name
Acetaminophen and Codeine Phosphate
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA089805
Marketed since
May 20, 2024
Listing expires
December 31, 2026
Pharmacologic class
Opioid Agonist

Active ingredients

Uses, dosage, side effects and warnings for Acetaminophen and Codeine Phosphate →

Package NDC codes (10)

Package NDCDescriptionSince
71335-2916-040 TABLET in 1 BOTTLE (71335-2916-0)Oct 28, 2025
71335-2916-16 TABLET in 1 BOTTLE (71335-2916-1)Oct 28, 2025
71335-2916-220 TABLET in 1 BOTTLE (71335-2916-2)Oct 28, 2025
71335-2916-330 TABLET in 1 BOTTLE (71335-2916-3)Oct 28, 2025
71335-2916-484 TABLET in 1 BOTTLE (71335-2916-4)Oct 28, 2025
71335-2916-515 TABLET in 1 BOTTLE (71335-2916-5)Oct 28, 2025
71335-2916-6120 TABLET in 1 BOTTLE (71335-2916-6)Oct 28, 2025
71335-2916-7100 TABLET in 1 BOTTLE (71335-2916-7)Oct 28, 2025
71335-2916-860 TABLET in 1 BOTTLE (71335-2916-8)Oct 28, 2025
71335-2916-990 TABLET in 1 BOTTLE (71335-2916-9)Oct 28, 2025

Other Acetaminophen and Codeine Phosphate products